Cilia Proteins Control Cerebellar Morphogenesis by Promoting Expansion of the Granule Progenitor Pool

Although human congenital cerebellar malformations are common, their molecular and developmental basis is still poorly understood. Recently, cilia-related gene deficiencies have been implicated in several congenital disorders that exhibit cerebellar abnormalities such as Joubert syndrome, Meckel-Gru...

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Publicado en:J Neurosci
Main Authors: Chizhikov, Victor V., Davenport, James, Zhang, Qihong, Shih, Evelyn Kim, Cabello, Olga A., Fuchs, Jannon L., Yoder, Bradley K., Millen, Kathleen J.
Formato: Artigo
Idioma:Inglês
Publicado: Society for Neuroscience 2007
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Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6672978/
https://ncbi.nlm.nih.gov/pubmed/17804638
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.5586-06.2007
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